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Fostamatinib: A Review in Chronic Immune Thrombocytopenia

机译:FOSTAMATINIB:慢性免疫血小板减少症综述

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Fostamatinib (Tavalisse(R); Tavlesse(R)) is the first spleen tyrosine kinase (Syk) inhibitor approved for the treatment of chronic immune thrombocytopenia (ITP) in adult patients who have had an insufficient response to previous treatment. By inhibiting Syk activation in macrophages, fostamatinib blocks autoantibody-mediated platelet phagocytosis. In the placebo-controlled phase III FIT1 and FIT2 trials, 24 weeks of oral fostamatinib therapy increased platelet count in previously treated adults with ITP. A significantly higher proportion of patients achieved stable response with fostamatinib than with placebo in FIT1, but not in FIT2; however, pooled analyses of the two studies showed that fostamatinib produced significantly higher stable and overall response rates than placebo. Interim findings from the ongoing FIT3 open-label extension study suggested that the efficacy of fostamatinib was maintained with long-term treatment (up to 62 months; median duration 6 months), including in patients receiving fostamatinib as second- or later-line treatment. Fostamatinib had a generally manageable tolerability profile in all three FIT studies, with no serious safety risks. Fostamatinib therefore provides an alternative treatment option for chronic ITP in adult patients with an insufficient response to previous treatment.
机译:福斯塔马蒂尼(塔瓦利斯(R);Tavlesse(R))是第一个被批准用于治疗慢性免疫性血小板减少症(ITP)的脾脏酪氨酸激酶(Syk)抑制剂,该病患者对之前的治疗反应不足。通过抑制巨噬细胞中的Syk活化,福斯塔马汀尼可阻断自身抗体介导的血小板吞噬作用。在安慰剂对照的III期FIT1和FIT2试验中,口服福斯塔马替尼24周后,先前接受ITP治疗的成年人的血小板计数增加。在FIT1中,福斯塔马汀尼获得稳定反应的患者比例显著高于安慰剂,但在FIT2中没有;然而,对这两项研究的汇总分析表明,福斯塔马替尼的稳定和总体应答率明显高于安慰剂。正在进行的FIT3开放标签扩展研究的中期结果表明,长期治疗(最长62个月;中位持续时间6个月)可以维持福斯塔马汀的疗效,包括接受福斯塔马汀二线或二线治疗的患者。在所有三项FIT研究中,福斯塔马蒂尼的耐受性总体可控,没有严重的安全风险。因此,福斯塔马蒂尼为之前治疗反应不足的成年慢性ITP患者提供了一种替代治疗方案。

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